ListarMED_Articles por tema "Rett syndrome"
Mostrando ítems 1-2 de 2
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Lack of MeCP2 leads to region-specific increase of doublecortin in the olfactory system
Springer (2019-05)The protein doublecortin is mainly expressed in migrating neuroblasts and immature neurons. The X-linked gene MECP2, associated to several neurodevelopmental disorders such as Rett syndrome, encodes the protein methyl-CpG-binding ... -
Male-specific features are reduced in Mecp2-null mice: analyses of vasopressinergic innervation, pheromone production and social behaviour
Springer (2020-08-04)Deficits in arginine vasopressin (AVP) and oxytocin (OT), two neuropeptides closely implicated in the modulation of social behaviours, have been reported in some early developmental disorders and autism spectrum disorders. ...